Job Summary Job Description JOB RESPONSIBILITIES (1) Collect and review Device Master Record (DMR) documents for Medline products subject to the regulatory requirements and project development plan; (2) Establish inspection criteria of new finished products, update
Job SummaryQA Specialist is responsible for quality assurance on the procedures of DMR and inspection criteria development and maintenance. Work closely with divisional QA and Asia stakeholders to ensure requirements are met under ISO13458 and CFR820.
Key Accountabilities Manage the daily facility-related operations of plan, including managing facility-related contracted services, building repair and maintenance, etc. Develop the facility maintenance plan, implement regular facility maintenance work on building, infrastructure, as well as utilities